Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc6 |
G |
T |
7: 45,679,680 (GRCm39) |
T9K |
probably benign |
Het |
Ankrd28 |
T |
C |
14: 31,429,177 (GRCm39) |
H925R |
probably damaging |
Het |
Antxrl |
A |
T |
14: 33,778,556 (GRCm39) |
T128S |
probably damaging |
Het |
Atosa |
A |
G |
9: 74,913,645 (GRCm39) |
M100V |
possibly damaging |
Het |
Atp8b5 |
T |
C |
4: 43,304,674 (GRCm39) |
Y62H |
probably damaging |
Het |
Bmpr2 |
G |
T |
1: 59,906,595 (GRCm39) |
V563L |
probably benign |
Het |
Btn1a1 |
A |
T |
13: 23,648,521 (GRCm39) |
L104Q |
probably damaging |
Het |
Caskin1 |
C |
G |
17: 24,726,154 (GRCm39) |
D1420E |
probably damaging |
Het |
Cdc14a |
A |
T |
3: 116,144,862 (GRCm39) |
I150N |
probably damaging |
Het |
Cdc26 |
C |
T |
4: 62,321,031 (GRCm39) |
R4Q |
probably damaging |
Het |
Cfap46 |
T |
C |
7: 139,236,496 (GRCm39) |
D160G |
probably damaging |
Het |
Cxcr4 |
A |
C |
1: 128,519,920 (GRCm39) |
|
probably null |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Dgat1 |
T |
C |
15: 76,387,493 (GRCm39) |
N317S |
possibly damaging |
Het |
Disp1 |
G |
A |
1: 182,880,589 (GRCm39) |
T228M |
possibly damaging |
Het |
Dixdc1 |
A |
C |
9: 50,614,656 (GRCm39) |
|
probably null |
Het |
Dnase1l2 |
C |
A |
17: 24,661,492 (GRCm39) |
|
probably benign |
Het |
Dsg2 |
T |
C |
18: 20,727,350 (GRCm39) |
|
probably null |
Het |
Duox2 |
A |
T |
2: 122,117,674 (GRCm39) |
F887I |
probably benign |
Het |
Duxf4 |
A |
G |
10: 58,071,344 (GRCm39) |
M290T |
probably benign |
Het |
Efcab6 |
T |
C |
15: 83,851,825 (GRCm39) |
D351G |
possibly damaging |
Het |
Ep400 |
A |
G |
5: 110,818,808 (GRCm39) |
V2621A |
probably damaging |
Het |
Epg5 |
G |
T |
18: 77,991,677 (GRCm39) |
V125F |
possibly damaging |
Het |
Ephb1 |
T |
C |
9: 101,800,783 (GRCm39) |
R953G |
probably damaging |
Het |
Etfdh |
G |
T |
3: 79,519,336 (GRCm39) |
Y272* |
probably null |
Het |
Fam117b |
A |
G |
1: 60,008,207 (GRCm39) |
E347G |
probably damaging |
Het |
Gfra3 |
A |
T |
18: 34,828,846 (GRCm39) |
C183S |
probably damaging |
Het |
Gmip |
A |
G |
8: 70,268,773 (GRCm39) |
D466G |
probably damaging |
Het |
Golga5 |
G |
A |
12: 102,450,740 (GRCm39) |
M464I |
probably benign |
Het |
Gpd1 |
A |
T |
15: 99,621,146 (GRCm39) |
Q320L |
possibly damaging |
Het |
H2-Oa |
G |
T |
17: 34,312,851 (GRCm39) |
D43Y |
probably damaging |
Het |
Hecw1 |
T |
A |
13: 14,520,623 (GRCm39) |
I205F |
probably damaging |
Het |
Ighv8-13 |
A |
G |
12: 115,728,973 (GRCm39) |
Y95H |
probably damaging |
Het |
Igkv6-20 |
T |
C |
6: 70,313,081 (GRCm39) |
M31V |
possibly damaging |
Het |
Itih1 |
T |
C |
14: 30,653,217 (GRCm39) |
D737G |
probably benign |
Het |
Kcnc4 |
G |
C |
3: 107,355,693 (GRCm39) |
H252D |
probably damaging |
Het |
Kcnj14 |
T |
A |
7: 45,468,921 (GRCm39) |
T195S |
probably damaging |
Het |
Limch1 |
A |
T |
5: 67,173,845 (GRCm39) |
D642V |
probably damaging |
Het |
Lrp2 |
T |
G |
2: 69,312,710 (GRCm39) |
D2526A |
possibly damaging |
Het |
Lrrc8a |
A |
G |
2: 30,146,565 (GRCm39) |
T460A |
possibly damaging |
Het |
Lrrn4cl |
A |
G |
19: 8,829,135 (GRCm39) |
T38A |
probably benign |
Het |
Lypd8 |
A |
T |
11: 58,277,629 (GRCm39) |
Q137L |
possibly damaging |
Het |
Mapkapk3 |
A |
G |
9: 107,137,262 (GRCm39) |
Y206H |
probably damaging |
Het |
Mrc1 |
G |
A |
2: 14,276,115 (GRCm39) |
G483D |
probably benign |
Het |
Mrpl35 |
C |
A |
6: 71,800,661 (GRCm39) |
|
probably benign |
Het |
Mycbp2 |
T |
A |
14: 103,497,665 (GRCm39) |
H936L |
probably benign |
Het |
Myh3 |
A |
T |
11: 66,978,312 (GRCm39) |
Y433F |
probably benign |
Het |
Napb |
C |
T |
2: 148,540,098 (GRCm39) |
|
probably null |
Het |
Nbeal1 |
C |
A |
1: 60,335,083 (GRCm39) |
Q2288K |
probably benign |
Het |
Ndst3 |
G |
A |
3: 123,465,301 (GRCm39) |
Q224* |
probably null |
Het |
Nkapd1 |
A |
G |
9: 50,518,971 (GRCm39) |
S214P |
possibly damaging |
Het |
Nkd2 |
A |
G |
13: 73,969,579 (GRCm39) |
S284P |
probably benign |
Het |
Or10a2 |
T |
C |
7: 106,673,343 (GRCm39) |
Y103H |
probably damaging |
Het |
Or5b12 |
A |
T |
19: 12,897,301 (GRCm39) |
V124E |
probably damaging |
Het |
Or6k2 |
G |
A |
1: 173,979,712 (GRCm39) |
S210N |
probably benign |
Het |
Or8h10 |
T |
C |
2: 86,809,035 (GRCm39) |
Y35C |
probably damaging |
Het |
Pcdhb8 |
A |
G |
18: 37,490,037 (GRCm39) |
T572A |
probably benign |
Het |
Pcdhb9 |
A |
G |
18: 37,535,115 (GRCm39) |
I370V |
probably benign |
Het |
Pcsk5 |
T |
G |
19: 17,558,631 (GRCm39) |
E592A |
possibly damaging |
Het |
Pigc |
T |
C |
1: 161,798,036 (GRCm39) |
V6A |
probably benign |
Het |
Pla2g6 |
T |
G |
15: 79,189,924 (GRCm39) |
I389L |
probably benign |
Het |
Pnliprp2 |
T |
C |
19: 58,751,874 (GRCm39) |
|
probably null |
Het |
Psmb11 |
T |
C |
14: 54,863,646 (GRCm39) |
V288A |
probably benign |
Het |
Rapgef5 |
A |
G |
12: 117,685,398 (GRCm39) |
|
probably null |
Het |
Rcn3 |
T |
C |
7: 44,732,720 (GRCm39) |
N316S |
probably damaging |
Het |
Rgs6 |
A |
G |
12: 83,112,738 (GRCm39) |
K183E |
probably damaging |
Het |
Rhoc |
A |
G |
3: 104,700,297 (GRCm39) |
|
probably null |
Het |
Serinc5 |
T |
C |
13: 92,844,616 (GRCm39) |
C453R |
probably damaging |
Het |
Slc14a1 |
A |
C |
18: 78,159,614 (GRCm39) |
M93R |
probably damaging |
Het |
Slc25a3 |
A |
T |
10: 90,958,090 (GRCm39) |
D83E |
probably damaging |
Het |
Slc36a3 |
T |
C |
11: 55,015,777 (GRCm39) |
Y459C |
probably benign |
Het |
Slc44a5 |
A |
T |
3: 153,944,800 (GRCm39) |
Y139F |
probably benign |
Het |
Stap2 |
C |
T |
17: 56,306,976 (GRCm39) |
V234M |
probably damaging |
Het |
Stard9 |
A |
G |
2: 120,544,231 (GRCm39) |
Y4450C |
probably damaging |
Het |
Taf6l |
C |
T |
19: 8,756,030 (GRCm39) |
R206Q |
probably benign |
Het |
Tbc1d23 |
C |
T |
16: 57,003,266 (GRCm39) |
V501I |
probably damaging |
Het |
Thap2 |
T |
C |
10: 115,208,751 (GRCm39) |
H123R |
probably damaging |
Het |
Tlx3 |
C |
A |
11: 33,152,432 (GRCm39) |
W221L |
probably benign |
Het |
Tmem262 |
T |
A |
19: 6,130,567 (GRCm39) |
|
probably null |
Het |
Tpmt |
C |
A |
13: 47,180,735 (GRCm39) |
R201S |
probably benign |
Het |
Trpm6 |
T |
C |
19: 18,831,655 (GRCm39) |
S1507P |
probably damaging |
Het |
Ttc9c |
T |
C |
19: 8,795,847 (GRCm39) |
E64G |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,640,790 (GRCm39) |
S13653T |
probably damaging |
Het |
Ugt3a1 |
G |
T |
15: 9,310,726 (GRCm39) |
W336L |
possibly damaging |
Het |
Vmn1r215 |
C |
A |
13: 23,260,633 (GRCm39) |
N224K |
probably benign |
Het |
Vmn2r59 |
C |
T |
7: 41,691,835 (GRCm39) |
|
probably null |
Het |
Wdfy3 |
A |
G |
5: 102,046,295 (GRCm39) |
S1853P |
possibly damaging |
Het |
Wdr36 |
A |
T |
18: 32,975,059 (GRCm39) |
Y137F |
possibly damaging |
Het |
Zdhhc17 |
T |
C |
10: 110,792,216 (GRCm39) |
D324G |
probably benign |
Het |
Zfp217 |
T |
C |
2: 169,961,497 (GRCm39) |
T277A |
probably benign |
Het |
Zfp451 |
A |
G |
1: 33,842,219 (GRCm39) |
|
probably benign |
Het |
Zfp709 |
TCGACG |
TCG |
8: 72,644,552 (GRCm39) |
|
probably benign |
Het |
Zfp871 |
T |
C |
17: 32,994,858 (GRCm39) |
S106G |
possibly damaging |
Het |
|
Other mutations in Spag17 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01096:Spag17
|
APN |
3 |
99,970,691 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01143:Spag17
|
APN |
3 |
99,846,614 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01329:Spag17
|
APN |
3 |
100,002,865 (GRCm39) |
missense |
probably benign |
0.16 |
IGL01393:Spag17
|
APN |
3 |
99,934,926 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01617:Spag17
|
APN |
3 |
100,016,824 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL01705:Spag17
|
APN |
3 |
99,930,046 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01928:Spag17
|
APN |
3 |
99,847,390 (GRCm39) |
splice site |
probably benign |
|
IGL01981:Spag17
|
APN |
3 |
99,966,149 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02435:Spag17
|
APN |
3 |
99,889,760 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL02452:Spag17
|
APN |
3 |
99,934,707 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02465:Spag17
|
APN |
3 |
99,983,187 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02615:Spag17
|
APN |
3 |
99,979,401 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02751:Spag17
|
APN |
3 |
99,918,110 (GRCm39) |
nonsense |
probably null |
|
IGL02803:Spag17
|
APN |
3 |
100,016,713 (GRCm39) |
missense |
probably benign |
|
IGL02898:Spag17
|
APN |
3 |
100,008,702 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03037:Spag17
|
APN |
3 |
99,979,486 (GRCm39) |
splice site |
probably null |
|
IGL03068:Spag17
|
APN |
3 |
99,987,521 (GRCm39) |
missense |
probably benign |
0.35 |
IGL03131:Spag17
|
APN |
3 |
99,918,075 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL03224:Spag17
|
APN |
3 |
99,918,156 (GRCm39) |
missense |
possibly damaging |
0.53 |
FR4342:Spag17
|
UTSW |
3 |
99,963,568 (GRCm39) |
small insertion |
probably benign |
|
FR4342:Spag17
|
UTSW |
3 |
99,963,565 (GRCm39) |
small insertion |
probably benign |
|
FR4548:Spag17
|
UTSW |
3 |
99,963,570 (GRCm39) |
small insertion |
probably benign |
|
FR4589:Spag17
|
UTSW |
3 |
99,963,574 (GRCm39) |
small insertion |
probably benign |
|
FR4589:Spag17
|
UTSW |
3 |
99,963,561 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Spag17
|
UTSW |
3 |
99,963,573 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Spag17
|
UTSW |
3 |
99,963,571 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Spag17
|
UTSW |
3 |
99,963,570 (GRCm39) |
small insertion |
probably benign |
|
N/A:Spag17
|
UTSW |
3 |
99,889,570 (GRCm39) |
splice site |
probably benign |
|
PIT4504001:Spag17
|
UTSW |
3 |
100,010,426 (GRCm39) |
critical splice acceptor site |
probably null |
|
PIT4514001:Spag17
|
UTSW |
3 |
99,920,527 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0107:Spag17
|
UTSW |
3 |
99,958,103 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0230:Spag17
|
UTSW |
3 |
100,014,143 (GRCm39) |
missense |
probably benign |
0.08 |
R0243:Spag17
|
UTSW |
3 |
99,992,684 (GRCm39) |
missense |
probably benign |
0.04 |
R0321:Spag17
|
UTSW |
3 |
100,008,719 (GRCm39) |
missense |
probably damaging |
0.99 |
R0375:Spag17
|
UTSW |
3 |
99,934,906 (GRCm39) |
missense |
probably benign |
|
R0417:Spag17
|
UTSW |
3 |
99,972,870 (GRCm39) |
missense |
probably benign |
0.11 |
R0490:Spag17
|
UTSW |
3 |
99,889,727 (GRCm39) |
missense |
probably damaging |
0.97 |
R0537:Spag17
|
UTSW |
3 |
100,032,618 (GRCm39) |
missense |
probably damaging |
0.98 |
R0714:Spag17
|
UTSW |
3 |
99,987,472 (GRCm39) |
missense |
probably damaging |
0.97 |
R0844:Spag17
|
UTSW |
3 |
99,912,101 (GRCm39) |
missense |
probably benign |
|
R0919:Spag17
|
UTSW |
3 |
99,979,259 (GRCm39) |
splice site |
probably benign |
|
R0926:Spag17
|
UTSW |
3 |
99,979,432 (GRCm39) |
missense |
probably benign |
|
R1037:Spag17
|
UTSW |
3 |
100,010,433 (GRCm39) |
missense |
probably benign |
0.01 |
R1075:Spag17
|
UTSW |
3 |
100,000,992 (GRCm39) |
missense |
probably damaging |
0.99 |
R1109:Spag17
|
UTSW |
3 |
99,934,667 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1213:Spag17
|
UTSW |
3 |
100,002,954 (GRCm39) |
missense |
probably benign |
0.01 |
R1221:Spag17
|
UTSW |
3 |
99,889,584 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1576:Spag17
|
UTSW |
3 |
99,846,679 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1586:Spag17
|
UTSW |
3 |
99,929,068 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1768:Spag17
|
UTSW |
3 |
99,934,668 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1782:Spag17
|
UTSW |
3 |
99,918,070 (GRCm39) |
missense |
probably benign |
0.02 |
R1789:Spag17
|
UTSW |
3 |
99,846,672 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1945:Spag17
|
UTSW |
3 |
99,847,298 (GRCm39) |
missense |
probably benign |
|
R2065:Spag17
|
UTSW |
3 |
99,920,524 (GRCm39) |
missense |
probably benign |
0.03 |
R2118:Spag17
|
UTSW |
3 |
99,956,556 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2265:Spag17
|
UTSW |
3 |
99,969,182 (GRCm39) |
splice site |
probably null |
|
R2266:Spag17
|
UTSW |
3 |
99,969,182 (GRCm39) |
splice site |
probably null |
|
R2267:Spag17
|
UTSW |
3 |
99,969,182 (GRCm39) |
splice site |
probably null |
|
R2268:Spag17
|
UTSW |
3 |
99,969,182 (GRCm39) |
splice site |
probably null |
|
R2271:Spag17
|
UTSW |
3 |
100,014,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R2389:Spag17
|
UTSW |
3 |
100,014,153 (GRCm39) |
missense |
probably benign |
0.27 |
R2420:Spag17
|
UTSW |
3 |
99,934,935 (GRCm39) |
missense |
probably benign |
|
R2422:Spag17
|
UTSW |
3 |
99,934,935 (GRCm39) |
missense |
probably benign |
|
R2423:Spag17
|
UTSW |
3 |
100,010,772 (GRCm39) |
missense |
probably benign |
|
R3407:Spag17
|
UTSW |
3 |
99,992,615 (GRCm39) |
missense |
probably benign |
0.09 |
R3801:Spag17
|
UTSW |
3 |
99,961,169 (GRCm39) |
missense |
possibly damaging |
0.53 |
R3856:Spag17
|
UTSW |
3 |
100,014,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R4021:Spag17
|
UTSW |
3 |
99,956,546 (GRCm39) |
missense |
probably benign |
0.00 |
R4022:Spag17
|
UTSW |
3 |
99,956,546 (GRCm39) |
missense |
probably benign |
0.00 |
R4408:Spag17
|
UTSW |
3 |
100,010,694 (GRCm39) |
missense |
probably benign |
|
R4468:Spag17
|
UTSW |
3 |
99,992,682 (GRCm39) |
missense |
probably damaging |
0.98 |
R4540:Spag17
|
UTSW |
3 |
99,995,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R4621:Spag17
|
UTSW |
3 |
100,010,559 (GRCm39) |
missense |
probably benign |
0.08 |
R4622:Spag17
|
UTSW |
3 |
100,010,559 (GRCm39) |
missense |
probably benign |
0.08 |
R4756:Spag17
|
UTSW |
3 |
100,010,701 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4797:Spag17
|
UTSW |
3 |
99,891,795 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4855:Spag17
|
UTSW |
3 |
99,970,649 (GRCm39) |
missense |
probably benign |
0.02 |
R4887:Spag17
|
UTSW |
3 |
99,958,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R4962:Spag17
|
UTSW |
3 |
99,934,939 (GRCm39) |
missense |
probably benign |
|
R5030:Spag17
|
UTSW |
3 |
99,992,657 (GRCm39) |
nonsense |
probably null |
|
R5042:Spag17
|
UTSW |
3 |
99,979,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R5074:Spag17
|
UTSW |
3 |
99,987,434 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5195:Spag17
|
UTSW |
3 |
100,008,704 (GRCm39) |
missense |
probably benign |
0.16 |
R5200:Spag17
|
UTSW |
3 |
99,970,787 (GRCm39) |
nonsense |
probably null |
|
R5267:Spag17
|
UTSW |
3 |
99,969,264 (GRCm39) |
missense |
probably damaging |
0.98 |
R5360:Spag17
|
UTSW |
3 |
100,016,726 (GRCm39) |
missense |
probably benign |
0.00 |
R5444:Spag17
|
UTSW |
3 |
99,963,468 (GRCm39) |
missense |
probably benign |
0.06 |
R5498:Spag17
|
UTSW |
3 |
100,010,661 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5503:Spag17
|
UTSW |
3 |
99,934,560 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5540:Spag17
|
UTSW |
3 |
99,963,588 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5547:Spag17
|
UTSW |
3 |
99,963,468 (GRCm39) |
missense |
probably benign |
0.06 |
R5575:Spag17
|
UTSW |
3 |
99,961,138 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5629:Spag17
|
UTSW |
3 |
99,987,435 (GRCm39) |
missense |
probably benign |
0.33 |
R5639:Spag17
|
UTSW |
3 |
99,963,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R5842:Spag17
|
UTSW |
3 |
99,846,566 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5976:Spag17
|
UTSW |
3 |
100,003,107 (GRCm39) |
nonsense |
probably null |
|
R6082:Spag17
|
UTSW |
3 |
100,031,501 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6254:Spag17
|
UTSW |
3 |
99,972,901 (GRCm39) |
missense |
probably benign |
0.03 |
R6321:Spag17
|
UTSW |
3 |
99,995,743 (GRCm39) |
missense |
probably benign |
0.05 |
R6446:Spag17
|
UTSW |
3 |
100,010,448 (GRCm39) |
missense |
probably benign |
|
R6687:Spag17
|
UTSW |
3 |
100,000,266 (GRCm39) |
missense |
probably benign |
0.07 |
R6853:Spag17
|
UTSW |
3 |
99,920,551 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6946:Spag17
|
UTSW |
3 |
99,911,999 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6953:Spag17
|
UTSW |
3 |
99,942,291 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7038:Spag17
|
UTSW |
3 |
99,891,925 (GRCm39) |
missense |
probably benign |
0.00 |
R7084:Spag17
|
UTSW |
3 |
99,846,586 (GRCm39) |
missense |
probably benign |
0.18 |
R7126:Spag17
|
UTSW |
3 |
100,008,751 (GRCm39) |
missense |
probably benign |
0.00 |
R7144:Spag17
|
UTSW |
3 |
99,934,717 (GRCm39) |
splice site |
probably null |
|
R7198:Spag17
|
UTSW |
3 |
100,002,888 (GRCm39) |
missense |
probably benign |
0.02 |
R7318:Spag17
|
UTSW |
3 |
99,847,299 (GRCm39) |
missense |
probably benign |
0.00 |
R7403:Spag17
|
UTSW |
3 |
99,846,691 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7409:Spag17
|
UTSW |
3 |
99,934,547 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7409:Spag17
|
UTSW |
3 |
99,941,475 (GRCm39) |
missense |
probably benign |
0.00 |
R7537:Spag17
|
UTSW |
3 |
99,846,563 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7609:Spag17
|
UTSW |
3 |
100,002,911 (GRCm39) |
nonsense |
probably null |
|
R7772:Spag17
|
UTSW |
3 |
99,987,434 (GRCm39) |
missense |
probably damaging |
0.98 |
R7842:Spag17
|
UTSW |
3 |
99,961,174 (GRCm39) |
missense |
probably benign |
0.18 |
R7963:Spag17
|
UTSW |
3 |
99,929,954 (GRCm39) |
missense |
probably benign |
0.02 |
R8168:Spag17
|
UTSW |
3 |
99,942,300 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8291:Spag17
|
UTSW |
3 |
99,968,166 (GRCm39) |
missense |
probably benign |
|
R8347:Spag17
|
UTSW |
3 |
99,934,957 (GRCm39) |
missense |
probably benign |
|
R8383:Spag17
|
UTSW |
3 |
99,992,708 (GRCm39) |
missense |
probably damaging |
0.98 |
R8474:Spag17
|
UTSW |
3 |
99,934,586 (GRCm39) |
missense |
probably benign |
0.00 |
R8528:Spag17
|
UTSW |
3 |
100,031,501 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8804:Spag17
|
UTSW |
3 |
99,874,506 (GRCm39) |
missense |
probably benign |
|
R8809:Spag17
|
UTSW |
3 |
99,889,738 (GRCm39) |
missense |
probably benign |
0.33 |
R8818:Spag17
|
UTSW |
3 |
99,920,543 (GRCm39) |
missense |
probably benign |
0.02 |
R8830:Spag17
|
UTSW |
3 |
100,032,751 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8890:Spag17
|
UTSW |
3 |
99,911,994 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9008:Spag17
|
UTSW |
3 |
99,934,942 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9095:Spag17
|
UTSW |
3 |
99,912,092 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9143:Spag17
|
UTSW |
3 |
99,934,906 (GRCm39) |
missense |
probably benign |
|
R9182:Spag17
|
UTSW |
3 |
99,966,158 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9211:Spag17
|
UTSW |
3 |
100,032,614 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R9344:Spag17
|
UTSW |
3 |
100,010,793 (GRCm39) |
missense |
probably benign |
0.01 |
R9354:Spag17
|
UTSW |
3 |
99,934,905 (GRCm39) |
missense |
probably benign |
|
R9527:Spag17
|
UTSW |
3 |
99,970,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R9658:Spag17
|
UTSW |
3 |
99,934,932 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9738:Spag17
|
UTSW |
3 |
99,934,526 (GRCm39) |
missense |
possibly damaging |
0.53 |
X0025:Spag17
|
UTSW |
3 |
100,008,767 (GRCm39) |
missense |
probably benign |
0.31 |
Z1088:Spag17
|
UTSW |
3 |
100,002,946 (GRCm39) |
missense |
probably benign |
0.09 |
Z1176:Spag17
|
UTSW |
3 |
99,920,309 (GRCm39) |
missense |
probably benign |
0.18 |
Z1177:Spag17
|
UTSW |
3 |
99,995,715 (GRCm39) |
missense |
probably damaging |
1.00 |
|